Inhibition of experimental diabetic cataract by topical administration of RS-verapamil hydrochloride

Aim: To investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats. Methods: Diabetes was induced in 69 male Sprague-Dawley rats by an intraperitoneal injection of streptozotocin (65 mg/kg body weight). One group (DV) of animals was treated by instillation of one dro...

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Published in:British journal of ophthalmology Vol. 88; no. 1; pp. 44 - 47
Main Authors: Ettl, A, Daxer, A, Göttinger, W, Schmid, E
Format: Journal Article
Language:English
Published: BMA House, Tavistock Square, London, WC1H 9JR BMJ Publishing Group Ltd 01-01-2004
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Abstract Aim: To investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats. Methods: Diabetes was induced in 69 male Sprague-Dawley rats by an intraperitoneal injection of streptozotocin (65 mg/kg body weight). One group (DV) of animals was treated by instillation of one drop of 0.2% RS-verapamil hydrochloride in both eyes three times daily for 8 weeks. The placebo treated group (D) received the vehicle solution only. After 8 weeks the lenses were removed, inspected, and photographed using bright and dark field illumination. The transmission of He-Ne laser light was measured in the optical axis of each lens in order to determine the turbidity coefficient (t) as a measure of central lens opacity. Following digital image analysis, the integrated density as a measure of central and mid-peripheral opacities was determined. Results: Lenses of both groups developed peripheral cortical opacities not affecting the optical axis. Advanced and paracentral cortical opacities were present in 10 (16.7%) of the placebo treated lenses (D) and two (3.8%) of the verapamil treated lenses (DV). Complete corticonuclear cataract developed in four (6.7%) of the lenses from group D but none of the lenses from group DV. The mean lens turbidity t was determined to be 0.019 (SEM 0.002) mm−1 (n  =  52) in the verapamil treated diabetic rats (DV) and 0.042 (0.008) mm−1 (n  =  60) in the placebo treated group (D). This difference was statistically significant (p  =  0.0054). The mean integrated density was 274.91 (22.5) in group D (n  =  60) and 196.28 (20.7) in group DV (n  =  37). This difference was also significant (p  =  0.0037). Conclusion: Verapamil eye drops 0.2% administered three times daily are effective in inhibiting the progression of lens opacities in streptozotocin diabetic rats.
AbstractList To investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats. Diabetes was induced in 69 male Sprague-Dawley rats by an intraperitoneal injection of streptozotocin (65 mg/kg body weight). One group (DV) of animals was treated by instillation of one drop of 0.2% RS-verapamil hydrochloride in both eyes three times daily for 8 weeks. The placebo treated group (D) received the vehicle solution only. After 8 weeks the lenses were removed, inspected, and photographed using bright and dark field illumination. The transmission of He-Ne laser light was measured in the optical axis of each lens in order to determine the turbidity coefficient (t) as a measure of central lens opacity. Following digital image analysis, the integrated density as a measure of central and mid-peripheral opacities was determined. Lenses of both groups developed peripheral cortical opacities not affecting the optical axis. Advanced and paracentral cortical opacities were present in 10 (16.7%) of the placebo treated lenses (D) and two (3.8%) of the verapamil treated lenses (DV). Complete corticonuclear cataract developed in four (6.7%) of the lenses from group D but none of the lenses from group DV. The mean lens turbidity t was determined to be 0.019 (SEM 0.002) mm(-1) (n = 52) in the verapamil treated diabetic rats (DV) and 0.042 (0.008) mm(-1) (n = 60) in the placebo treated group (D). This difference was statistically significant (p = 0.0054). The mean integrated density was 274.91 (22.5) in group D (n = 60) and 196.28 (20.7) in group DV (n = 37). This difference was also significant (p = 0.0037). Verapamil eye drops 0.2% administered three times daily are effective in inhibiting the progression of lens opacities in streptozotocin diabetic rats.
Aim: To investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats. Methods: Diabetes was induced in 69 male Sprague-Dawley rats by an intraperitoneal injection of streptozotocin (65 mg/kg body weight). One group (DV) of animals was treated by instillation of one drop of 0.2% RS-verapamil hydrochloride in both eyes three times daily for 8 weeks. The placebo treated group (D) received the vehicle solution only. After 8 weeks the lenses were removed, inspected, and photographed using bright and dark field illumination. The transmission of He-Ne laser light was measured in the optical axis of each lens in order to determine the turbidity coefficient (t) as a measure of central lens opacity. Following digital image analysis, the integrated density as a measure of central and mid-peripheral opacities was determined. Results: Lenses of both groups developed peripheral cortical opacities not affecting the optical axis. Advanced and paracentral cortical opacities were present in 10 (16.7%) of the placebo treated lenses (D) and two (3.8%) of the verapamil treated lenses (DV). Complete corticonuclear cataract developed in four (6.7%) of the lenses from group D but none of the lenses from group DV. The mean lens turbidity t was determined to be 0.019 (SEM 0.002) mm−1 (n  =  52) in the verapamil treated diabetic rats (DV) and 0.042 (0.008) mm−1 (n  =  60) in the placebo treated group (D). This difference was statistically significant (p  =  0.0054). The mean integrated density was 274.91 (22.5) in group D (n  =  60) and 196.28 (20.7) in group DV (n  =  37). This difference was also significant (p  =  0.0037). Conclusion: Verapamil eye drops 0.2% administered three times daily are effective in inhibiting the progression of lens opacities in streptozotocin diabetic rats.
Aim: To investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats. Methods: Diabetes was induced in 69 male Sprague-Dawley rats by an intraperitoneal injection of streptozotocin (65 mg/kg body weight). One group (DV) of animals was treated by instillation of one drop of 0.2% RS-verapamil hydrochloride in both eyes three times daily for 8 weeks. The placebo treated group (D) received the vehicle solution only. After 8 weeks the lenses were removed, inspected, and photographed using bright and dark field illumination. The transmission of He-Ne laser light was measured in the optical axis of each lens in order to determine the turbidity coefficient (t) as a measure of central lens opacity. Following digital image analysis, the integrated density as a measure of central and mid-peripheral opacities was determined. Results: Lenses of both groups developed peripheral cortical opacities not affecting the optical axis. Advanced and paracentral cortical opacities were present in 10 (16.7%) of the placebo treated lenses (D) and two (3.8%) of the verapamil treated lenses (DV). Complete corticonuclear cataract developed in four (6.7%) of the lenses from group D but none of the lenses from group DV. The mean lens turbidity t was determined to be 0.019 (SEM 0.002) mm -1 (n = 52) in the verapamil treated diabetic rats (DV) and 0.042 (0.008) mm-1 (n = 60) in the placebo treated group (D). This difference was statistically significant (p = 0.0054). The mean integrated density was 274.91 (22.5) in group D (n = 60) and 196.28 (20.7) in group DV (n = 37). This difference was also significant (p = 0.0037). Conclusion: Verapamil eye drops 0.2% administered three times daily are effective in inhibiting the progression of lens opacities in streptozotocin diabetic rats.
AIMTo investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats.METHODSDiabetes was induced in 69 male Sprague-Dawley rats by an intraperitoneal injection of streptozotocin (65 mg/kg body weight). One group (DV) of animals was treated by instillation of one drop of 0.2% RS-verapamil hydrochloride in both eyes three times daily for 8 weeks. The placebo treated group (D) received the vehicle solution only. After 8 weeks the lenses were removed, inspected, and photographed using bright and dark field illumination. The transmission of He-Ne laser light was measured in the optical axis of each lens in order to determine the turbidity coefficient (t) as a measure of central lens opacity. Following digital image analysis, the integrated density as a measure of central and mid-peripheral opacities was determined.RESULTSLenses of both groups developed peripheral cortical opacities not affecting the optical axis. Advanced and paracentral cortical opacities were present in 10 (16.7%) of the placebo treated lenses (D) and two (3.8%) of the verapamil treated lenses (DV). Complete corticonuclear cataract developed in four (6.7%) of the lenses from group D but none of the lenses from group DV. The mean lens turbidity t was determined to be 0.019 (SEM 0.002) mm(-1) (n = 52) in the verapamil treated diabetic rats (DV) and 0.042 (0.008) mm(-1) (n = 60) in the placebo treated group (D). This difference was statistically significant (p = 0.0054). The mean integrated density was 274.91 (22.5) in group D (n = 60) and 196.28 (20.7) in group DV (n = 37). This difference was also significant (p = 0.0037).CONCLUSIONVerapamil eye drops 0.2% administered three times daily are effective in inhibiting the progression of lens opacities in streptozotocin diabetic rats.
Aim: To investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats. Methods: Diabetes was induced in 69 male Sprague-Dawley rats by an intraperitoneal injection of streptozotocin (65 mg/kg body weight). One group (DV) of animals was treated by instillation of one drop of 0.2% RS-verapamil hydrochloride in both eyes three times daily for 8 weeks. The placebo treated group (D) received the vehicle solution only. After 8 weeks the lenses were removed, inspected, and photographed using bright and dark field illumination. The transmission of He-Ne laser light was measured in the optical axis of each lens in order to determine the turbidity coefficient (t) as a measure of central lens opacity. Following digital image analysis, the integrated density as a measure of central and mid-peripheral opacities was determined. Results: Lenses of both groups developed peripheral cortical opacities not affecting the optical axis. Advanced and paracentral cortical opacities were present in 10 (16.7%) of the placebo treated lenses (D) and two (3.8%) of the verapamil treated lenses (DV). Complete corticonuclear cataract developed in four (6.7%) of the lenses from group D but none of the lenses from group DV. The mean lens turbidity t was determined to be 0.019 (SEM 0.002) mm −1 (n  =  52) in the verapamil treated diabetic rats (DV) and 0.042 (0.008) mm −1 (n  =  60) in the placebo treated group (D). This difference was statistically significant (p  =  0.0054). The mean integrated density was 274.91 (22.5) in group D (n  =  60) and 196.28 (20.7) in group DV (n  =  37). This difference was also significant (p  =  0.0037). Conclusion: Verapamil eye drops 0.2% administered three times daily are effective in inhibiting the progression of lens opacities in streptozotocin diabetic rats.
Audience Professional
Academic
Author Daxer, A
Ettl, A
Göttinger, W
Schmid, E
AuthorAffiliation 1 Department of Ophthalmology, University of Innsbruck, Austria
3 Eye Center, Linz, Austria
2 Department of Neuro-Ophthalmology, Oculoplastic and Orbital Surgery, Central Hospital, Pölten, Austria
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Issue 1
Keywords Endocrinopathy
Human
Cataract
Chemoprophylaxis
Diabetes mellitus
Calcium antagonist
Prevention
Eye disease
Lens disease
Aralkylamine
Verapamil
Anterior segment disease
Topical administration
Language English
License CC BY 4.0
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Notes Correspondence to: Armin Ettl, MD, PhD Neuro-Ophthalmology, Zentraltrankenhaus Postfach 176, A-3100 St Pölten, Austria; a.ettl@kh-st-poelten.at
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Preliminary results of this study were presented at the annual meetings of the AER in Granada in 1993 and the ARVO in Fort Lauderdale in 1995.
Correspondence to: …Armin Ettl, MD, PhD …Neuro-Ophthalmology, Zentraltrankenhaus Postfach 176, A-3100 St Pölten, Austria; a.ettl@kh-st-poelten.at
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Snippet Aim: To investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats. Methods: Diabetes was induced in 69 male Sprague-Dawley...
To investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats. Diabetes was induced in 69 male Sprague-Dawley rats by an...
AIMTo investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats.METHODSDiabetes was induced in 69 male Sprague-Dawley rats by...
Aim: To investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats. Methods: Diabetes was induced in 69 male Sprague-Dawley...
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StartPage 44
SubjectTerms Animals
Associated diseases and complications
Biological and medical sciences
Calcium Channel Blockers - therapeutic use
Care and treatment
Cataract
Cataract - etiology
Cataract - prevention & control
Clinical Science - Scientific Reports
diabetes
Diabetes Mellitus, Experimental - complications
Diabetes. Impaired glucose tolerance
Disease Progression
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Image Processing, Computer-Assisted - methods
Lens diseases
Male
Medical sciences
Ophthalmic Solutions
Ophthalmology
Rats
Rats, Sprague-Dawley
verapamil
Verapamil - therapeutic use
Title Inhibition of experimental diabetic cataract by topical administration of RS-verapamil hydrochloride
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